Merck Group is inviting applications for the position of Senior Analyst โ Clinical Trial Coordinator in Bangalore, Karnataka, India. This is an excellent opportunity for clinical research professionals with experience in clinical operations, trial coordination, ICH-GCP guidelines, and clinical trial administration.
The role is part of the Local-Regional Studies Support Office and supports the smooth execution of local and regional clinical studies. Candidates with a scientific background and 1โ2 years of clinical research experience are encouraged to apply.
Job ID: 303686
Job Title: Senior Analyst โ Clinical Trial Coordinator
Company: Merck Group
Location: Bangalore, Karnataka, India
Work Mode: Hybrid
Job Type: Full-Time
Experience: 1โ2 Years
About Merck Group
Merck Group is a global science and technology organization operating across Healthcare, Life Science, and Electronics. Through innovation, scientific research, and advanced technologies, the company works to improve and prolong lives.
Within its Healthcare business, Merck focuses on developing medicines, intelligent devices, and innovative healthcare technologies across therapeutic areas including Oncology, Neurology, and Fertility.
Joining Merck offers clinical research professionals the opportunity to work in a diverse, international environment while contributing to global healthcare and clinical development activities.
Senior Analyst โ Clinical Trial Coordinator Job Responsibilities
As a Clinical Trial Coordinator, you will support clinical trial teams and help ensure that clinical studies operate efficiently, accurately, and in compliance with applicable processes and regulations.
Key responsibilities may include:
- Support the coordination and execution of local and regional clinical studies.
- Assist clinical trial teams with day-to-day clinical operations activities.
- Support clinical trial budget tracking and invoice management.
- Coordinate administrative and operational activities associated with clinical studies.
- Assist with quality issue tracking and follow-up activities.
- Support regulatory reporting oversight and documentation processes.
- Help maintain accurate clinical trial records and study-related documentation.
- Work closely with internal cross-functional teams and stakeholders.
- Ensure activities are performed in accordance with applicable processes and quality standards.
- Support compliance with ICH-GCP guidelines and clinical research requirements.
- Manage multiple tasks while maintaining accuracy and meeting established deadlines.
- Participate in the continuous improvement of clinical operations processes.
- Collaborate effectively within international and multicultural teams.
This Clinical Trial Coordinator job in Bangalore offers an opportunity to develop expertise in global clinical development and clinical operations.
Qualifications and Eligibility Criteria
Candidates applying for the Senior Analyst โ Clinical Trial Coordinator position at Merck Group should meet the following requirements:
Educational Qualification
- Bachelor’s degree or equivalent qualification in a scientific or relevant field.
Candidates without a bachelor’s degree may also be considered if they possess:
- A minimum of three years of relevant professional experience, and
- Additional qualifications demonstrating knowledge of clinical research fundamentals.
Experience
- 1โ2 years of experience in a clinical research-related role is preferred.
- Experience in clinical operations, clinical trial coordination, or clinical research administration can be beneficial.
Required Skills
Candidates should have:
- Foundational knowledge of clinical research and clinical operations.
- Understanding of ICH-GCP guidelines.
- Knowledge of clinical trial coordination processes.
- Strong organizational and administrative skills.
- Excellent attention to detail.
- Ability to manage high-volume tasks effectively.
- Good written and verbal communication skills in English.
- Proficiency in office productivity tools, including:
- Spreadsheet software
- Word processing software
- Presentation software
- Familiarity with Clinical Trial Management Systems (CTMS) is an advantage.
- Ability to work independently and collaboratively.
- Comfort working in a global and multicultural matrix environment.
- A proactive attitude and willingness to continuously learn.
Why Join Merck Group?
Working at Merck provides an opportunity to become part of a global organization focused on innovation, science, technology, and human progress.
Employees may benefit from:
- Opportunities for professional development and career growth.
- Exposure to global clinical development operations.
- Experience working with international and cross-functional teams.
- An inclusive and diverse working environment.
- Opportunities to build expertise in clinical research and clinical operations.
- Flexible and hybrid working opportunities, depending on business requirements.
- The opportunity to contribute to healthcare innovations that impact patients worldwide.
Who Should Apply?
This role may be suitable for professionals searching for:
- Clinical Trial Coordinator jobs in Bangalore
- Clinical Research jobs in Bangalore
- Clinical Operations jobs in India
- Clinical Trial Assistant jobs
- Clinical Study Coordinator jobs
- Clinical Project Coordinator jobs
- CTMS-related jobs
- ICH-GCP clinical research jobs
- Healthcare and pharmaceutical industry jobs
Candidates with a scientific education and experience in clinical research administration or clinical operations are encouraged to explore this opportunity.
Job Location
Bangalore, Karnataka, India
Work Arrangement: Hybrid
Employment Type: Full-Time
Estimated Salary
The salary for the Senior Analyst โ Clinical Trial Coordinator role at Merck Group may vary depending on the candidate’s experience, qualifications, skills, and internal compensation structure.
Estimated Salary Range: โน6,00,000 โ โน10,00,000 per annum.
Note: The salary range above is an estimate provided for informational purposes and is not an official compensation disclosure from Merck Group.
How to Apply
